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- PDB-4i1n: R104A-ca1697 nanobody binding to the binary DHFR.folate complex -

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Basic information

Entry
Database: PDB / ID: 4i1n
TitleR104A-ca1697 nanobody binding to the binary DHFR.folate complex
Components
  • Dihydrofolate reductase
  • Protein ca1697 (nanobody)
KeywordsOXIDOREDUCTASE/IMMUNE SYSTEM / alpha/beta fold / immunoglobulin fold / reductase / NADPH / folate derivatives / hydride transfer / OXIDOREDUCTASE-IMMUNE SYSTEM complex
Function / homology
Function and homology information


methotrexate binding / dihydrofolic acid binding / response to methotrexate / dihydrofolate metabolic process / NADP+ binding / folic acid binding / folic acid metabolic process / glycine biosynthetic process / dihydrofolate reductase / dihydrofolate reductase activity ...methotrexate binding / dihydrofolic acid binding / response to methotrexate / dihydrofolate metabolic process / NADP+ binding / folic acid binding / folic acid metabolic process / glycine biosynthetic process / dihydrofolate reductase / dihydrofolate reductase activity / NADPH binding / tetrahydrofolate biosynthetic process / one-carbon metabolic process / NADP binding / response to xenobiotic stimulus / response to antibiotic / cytosol
Similarity search - Function
Dihydrofolate Reductase, subunit A / Dihydrofolate Reductase, subunit A / Dihydrofolate reductase / Dihydrofolate reductase conserved site / Dihydrofolate reductase (DHFR) domain signature. / Dihydrofolate reductase domain / Dihydrofolate reductase / Dihydrofolate reductase (DHFR) domain profile. / Dihydrofolate reductase-like domain superfamily / Immunoglobulins ...Dihydrofolate Reductase, subunit A / Dihydrofolate Reductase, subunit A / Dihydrofolate reductase / Dihydrofolate reductase conserved site / Dihydrofolate reductase (DHFR) domain signature. / Dihydrofolate reductase domain / Dihydrofolate reductase / Dihydrofolate reductase (DHFR) domain profile. / Dihydrofolate reductase-like domain superfamily / Immunoglobulins / Immunoglobulin-like / Sandwich / 3-Layer(aba) Sandwich / Mainly Beta / Alpha Beta
Similarity search - Domain/homology
FOLIC ACID / Dihydrofolate reductase
Similarity search - Component
Biological speciesEscherichia coli (E. coli)
lama glama (llama)
MethodX-RAY DIFFRACTION / MOLECULAR REPLACEMENT / Resolution: 1.888 Å
AuthorsOyen, D. / Steyaert, J. / Barlow, J.N.
CitationJournal: To be Published
Title: Exploring an alternative antibody interaction mechanism
Authors: Oyen, D. / Steyaert, J. / Barlow, J.N.
History
DepositionNov 21, 2012Deposition site: RCSB / Processing site: PDBJ
Revision 1.0Nov 27, 2013Provider: repository / Type: Initial release

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Structure visualization

Structure viewerMolecule:
MolmilJmol/JSmol

Downloads & links

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Assembly

Deposited unit
A: Dihydrofolate reductase
B: Protein ca1697 (nanobody)
hetero molecules


Theoretical massNumber of molelcules
Total (without water)33,2013
Polymers32,7602
Non-polymers4411
Water5,441302
1


  • Idetical with deposited unit
  • defined by author
TypeNameSymmetry operationNumber
identity operation1_555x,y,z1
Unit cell
Length a, b, c (Å)49.267, 55.642, 119.213
Angle α, β, γ (deg.)90.00, 90.00, 90.00
Int Tables number19
Space group name H-MP212121

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Components

#1: Protein Dihydrofolate reductase /


Mass: 18019.340 Da / Num. of mol.: 1
Source method: isolated from a genetically manipulated source
Source: (gene. exp.) Escherichia coli (E. coli) / Strain: K12 / Gene: folA, tmrA, b0048, JW0047 / Production host: Escherichia coli (E. coli) / References: UniProt: P0ABQ4, dihydrofolate reductase
#2: Antibody Protein ca1697 (nanobody)


Mass: 14740.489 Da / Num. of mol.: 1 / Mutation: R104A
Source method: isolated from a genetically manipulated source
Source: (gene. exp.) lama glama (llama) / Production host: Escherichia coli (E. coli)
#3: Chemical ChemComp-FOL / FOLIC ACID / Folate


Mass: 441.397 Da / Num. of mol.: 1 / Source method: obtained synthetically / Formula: C19H19N7O6
#4: Water ChemComp-HOH / water / Water


Mass: 18.015 Da / Num. of mol.: 302 / Source method: isolated from a natural source / Formula: H2O
Sequence detailsRESIDUE 104 ALA OF ENTITY 2 REPRESENT ENGINEERED MUTATION (R104A)

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Experimental details

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Experiment

ExperimentMethod: X-RAY DIFFRACTION / Number of used crystals: 1

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Sample preparation

CrystalDensity Matthews: 2.49 Å3/Da / Density % sol: 50.68 %
Crystal growTemperature: 298 K / Method: vapor diffusion, hanging drop / pH: 6.5
Details: 30% v/v PEG 200, 5% w/v PEG 3000, 100mM MES Sodium Salt, pH 6.5, VAPOR DIFFUSION, HANGING DROP, temperature 298K

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Data collection

DiffractionMean temperature: 100 K
Diffraction sourceSource: ROTATING ANODE / Type: RIGAKU MICROMAX-007 HF / Wavelength: 1.5418 Å
DetectorType: RIGAKU SATURN 944+ / Detector: CCD / Date: Apr 13, 2012
RadiationMonochromator: graded multilayer monochromator / Protocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray
Radiation wavelengthWavelength: 1.5418 Å / Relative weight: 1
ReflectionResolution: 1.888→20 Å / Num. all: 26802 / Num. obs: 26266 / % possible obs: 98 % / Observed criterion σ(F): 0 / Observed criterion σ(I): 2 / Biso Wilson estimate: 23.23 Å2
Reflection shellResolution: 1.9→1.93 Å / % possible all: 98.2

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Processing

Software
NameVersionClassification
HKL-3000data collection
PHASERphasing
PHENIX(phenix.refine: 1.7.3_928)refinement
HKL-3000data reduction
HKL-3000data scaling
RefinementMethod to determine structure: MOLECULAR REPLACEMENT / Resolution: 1.888→19.596 Å / Occupancy max: 1 / Occupancy min: 0 / FOM work R set: 0.8347 / SU ML: 0.19 / σ(F): 1.34 / Phase error: 22.82 / Stereochemistry target values: ML
RfactorNum. reflection% reflection
Rfree0.2139 1318 5.05 %
Rwork0.1773 --
obs0.1793 26116 96.53 %
all-26266 -
Solvent computationShrinkage radii: 0.9 Å / VDW probe radii: 1.11 Å / Solvent model: FLAT BULK SOLVENT MODEL
Displacement parametersBiso max: 96.04 Å2 / Biso mean: 28.294 Å2 / Biso min: 6.06 Å2
Baniso -1Baniso -2Baniso -3
1-3.8755 Å2-0 Å20 Å2
2---5.1182 Å2-0 Å2
3---1.2426 Å2
Refinement stepCycle: LAST / Resolution: 1.888→19.596 Å
ProteinNucleic acidLigandSolventTotal
Num. atoms2233 0 32 302 2567
Refine LS restraints
Refine-IDTypeDev idealNumber
X-RAY DIFFRACTIONf_bond_d0.0072343
X-RAY DIFFRACTIONf_angle_d1.1033189
X-RAY DIFFRACTIONf_dihedral_angle_d14.52850
X-RAY DIFFRACTIONf_chiral_restr0.073341
X-RAY DIFFRACTIONf_plane_restr0.005414
LS refinement shell

Refine-ID: X-RAY DIFFRACTION / Total num. of bins used: 9

Resolution (Å)Rfactor RfreeNum. reflection RfreeRfactor RworkNum. reflection RworkNum. reflection all% reflection obs (%)
1.8878-1.96340.25621210.21342472259388
1.9634-2.05260.29211280.19652791291998
2.0526-2.16070.23591480.18092745289398
2.1607-2.29590.22061420.18422791293399
2.2959-2.47280.24081570.19152779293698
2.4728-2.72110.25371450.19052787293298
2.7211-3.11350.22021770.1842793297098
3.1135-3.91750.19261470.16472804295197
3.9175-19.59670.17641530.16222836298994
Refinement TLS params.

Method: refined / Refine-ID: X-RAY DIFFRACTION

IDL112)L122)L132)L222)L232)L332)S11 (Å °)S12 (Å °)S13 (Å °)S21 (Å °)S22 (Å °)S23 (Å °)S31 (Å °)S32 (Å °)S33 (Å °)T112)T122)T132)T222)T232)T332)Origin x (Å)Origin y (Å)Origin z (Å)
18.1552-0.3737-3.11122.5426-0.03585.162-0.4248-0.3023-0.31720.46160.0832-0.47030.33250.20650.29210.27840.0274-0.06520.15430.01770.209347.996445.281320.753
20.24250.4229-0.14731.91120.46870.53850.12440.0046-0.1420.07360.0179-0.1466-0.1156-0.0513-0.10330.23810.0267-0.0510.19070.04460.269950.620755.752812.8461
37.4213-1.1146-3.28973.1288-2.12967.2683-0.09510.1836-0.2339-0.349-0.00430.24520.3183-0.31570.1580.1876-0.0245-0.03180.18810.00330.169340.330445.9499.9457
42.1823-0.3415-0.6712.9608-0.18362.1977-0.0185-0.07240.02760.7904-0.06730.620.009-0.34780.03460.2929-0.00970.10280.22770.01960.23133.747454.384723.2749
50.4351-0.6799-0.38171.18581.04261.84280.0976-0.1074-0.00630.7616-0.0379-0.28090.0938-0.1224-0.09630.44-0.0142-0.01690.18310.01680.144244.827844.880824.543
62.730.6939-1.18061.8358-0.4762.6937-0.09970.00570.12430.6507-0.0227-0.82130.19390.36610.17160.35510.0582-0.14050.2480.00350.350555.523548.909221.519
71.24440.3486-0.89660.5996-0.76575.204-0.10330.00160.07730.52660.2592-0.28780.1887-0.0912-0.09480.40790.0387-0.0540.18710.00350.212649.84735.087517.1533
81.12270.62-0.00123.09170.22931.7275-0.11250.0976-0.0097-0.16860.2079-0.38320.4848-0.2242-0.0890.25240.00910.00240.16930.02930.187849.709441.750310.7884
91.30180.3554-0.54241.8277-1.13168.1301-0.16050.0850.26120.15140.00130.0756-0.34230.37850.18770.11390.0013-0.01680.17550.0290.247649.289782.69441.2716
100.73590.3370.2970.6363-0.28862.0063-0.10480.00090.0701-0.064-0.1647-0.1243-0.04690.45120.26340.1792-0.0055-0.00650.23590.08360.284153.037479.27293.505
111.2040.03130.21022.3939-0.24922.6434-0.0535-0.12880.08270.27950.1175-0.073-0.2424-0.1377-0.03760.12190.0182-0.00040.16030.0380.173348.021372.870411.5779
124.8775-3.24281.25573.1248-0.54420.3829-0.22710.1910.37360.06570.12530.1318-0.105-0.13250.1010.1268-0.00380.00150.19930.06990.268438.980374.19631.522
132.5640.88250.49181.5991.2362.9445-0.25120.29970.20740.1994-0.0549-0.20210.1280.3710.29140.12320.0309-0.01560.14160.01920.221350.995765.01415.9266
141.5123-1.05690.49872.135-0.52944.72730.0203-0.0484-0.1236-0.02360.1324-0.04830.1071-0.0082-0.1380.0907-0.00590.00530.19230.03780.191751.696671.75011.033
151.6574-0.5211-0.1851.7128-2.35613.7575-0.08130.22330.1535-0.15330.19430.01980.1138-0.4788-0.14090.1464-0.0415-0.02510.2140.05480.256543.718677.8613-2.771
165.2882-0.59040.01295.84080.65084.5534-0.1192-0.34490.17750.05540.12190.688-0.0918-0.52650.00710.14050.00620.01770.23280.04260.253539.264166.89329.8149
179.00453.2732-0.38673.6365-2.94853.24170.0201-0.60850.47530.1722-0.14360.4621-0.2191-0.19260.27650.2233-0.00810.00590.2831-0.01120.268241.402778.536812.416
187.842-0.10260.64557.47142.82081.9719-0.07810.73830.5762-0.590.05990.0725-0.4859-0.41160.01830.197-0.0276-0.04230.31120.10680.316844.077885.4528-7.5465
Refinement TLS group
IDRefine-IDRefine TLS-IDSelection details
1X-RAY DIFFRACTION1chain 'A' and (resseq 1:12)
2X-RAY DIFFRACTION2chain 'A' and (resseq 13:24)
3X-RAY DIFFRACTION3chain 'A' and (resseq 25:35)
4X-RAY DIFFRACTION4chain 'A' and (resseq 36:96)
5X-RAY DIFFRACTION5chain 'A' and (resseq 97:115)
6X-RAY DIFFRACTION6chain 'A' and (resseq 116:129)
7X-RAY DIFFRACTION7chain 'A' and (resseq 130:141)
8X-RAY DIFFRACTION8chain 'A' and (resseq 142:159)
9X-RAY DIFFRACTION9chain 'B' and (resseq 1:17)
10X-RAY DIFFRACTION10chain 'B' and (resseq 18:24)
11X-RAY DIFFRACTION11chain 'B' and (resseq 25:39)
12X-RAY DIFFRACTION12chain 'B' and (resseq 40:52)
13X-RAY DIFFRACTION13chain 'B' and (resseq 53:60)
14X-RAY DIFFRACTION14chain 'B' and (resseq 61:83)
15X-RAY DIFFRACTION15chain 'B' and (resseq 84:99)
16X-RAY DIFFRACTION16chain 'B' and (resseq 100:113)
17X-RAY DIFFRACTION17chain 'B' and (resseq 114:120)
18X-RAY DIFFRACTION18chain 'B' and (resseq 121:128)

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